N4-Acetylcytosine

Basic information

  • Product Name:N4-Acetylcytosine
  • CasNo.:14631-20-0
  • MF:C6H7N3O2
  • MW:153.14

Physical and Chemical Properties

  • Boiling Point:>300 °C(lit.)
  • Packing:25kg/drum or as required by customer
  • Throughput:
Inquiry

Product Details

CasNo: 14631-20-0

MF: C6H7N3O2

Packing: 25kg/drum or as required by customer

Cost-effective and customizable N4-Acetylcytosine 14631-20-0 factory

ynonyms: N4-Acetylcytosine;

Molecular Formula: C6H7N3O2

Molecular Weight: 153.14 

CAS Number14631-20-0

Item

Specification

Appearance

White to Off-White powder

Loss on drying,%

≤0.5

Residue on ignition,%

≤0.10

Assay (HPLC),%

≥98.0

Acetic acid,%

≤0.5

Other single impurities,%

≤0.5

total impurities,%

≤1.0

Characteristics: White to Off-White powder. It is slightly soluble in acetone, methanol and dimethyl sulfoxide and insoluble in water.

N4-Acetylcytosine(Cas 14631-20-0) Usage

Used for the synthesis of pharmaceutical intermediates, raw materials of photoreceptors, pyrimidine anti-tumor drugs and anti-AIDS drugs.

Storage: Store in a tightly closed container. Maintain in a cool and dry area.

Package: 25kg/drum or as required by customer.

Expiration Date: 2 years

14631-20-0 Relevant articles

Synthesis, physicochemical characteristics, and biocompatibility of self-assemble polymers bearing guanine, cytosine, uracil, and thymine moieties

Kim, Jin Chul,Kim, Mihee,Jung, Jungwoon,Lee, Jinseok,Ree, Brian J.,Kim, Heesoo,Kim, Ik Jung,Kim, Jung Ran,Ree, Moonhor

, p. 1151 - 1160 (2015)

We synthesized chemically well-defined b...

-

Codington et al.

, p. 5164 (1958)

-

Synthesis of N4-β-D-glycoside cytosines and sugar N 4-acetylcytosin-1-ylmethylhydrazones as antiviral agents

Ali, Omar M.,Amer, Hamada H.,Abdel-Rahman, Adel A.-H.

, p. 281 - 283 (2007)

Reaction of monosaccharide aldoses with ...

Discovery of α-aminoazaheterocycle-methylglyoxal adducts as a new class of high-affinity inhibitors of cystic fibrosis transmembrane conductance regulator chloride channels

Routaboul, Christel,Norez, Caroline,Melin, Patricia,Molina, Marie-Carmen,Boucherle, Benjamin,Bossard, Florian,Noel, Sabrina,Robert, Renaud,Gauthier, Chantal,Becq, Frederic,Decout, Jean-Luc

, p. 1023 - 1035 (2007)

The cystic fibrosis transmembrane conduc...

N -Glycosylation with sulfoxide donors for the synthesis of peptidonucleosides

Beau, Jean-Marie,Beretta, Margaux,Dr?ge, Thomas,Es-Sayed, Mazen,Nicolas, Lionel,Norsikian, Stéphanie,Rouchaud, Emilie,Vors, Jean-Pierre

supporting information, p. 4285 - 4291 (2021/05/31)

The synthesis of glycopyranosyl nucleosi...

Preparation method for synthesizing palbociclib intermediate and method for synthesizing palbociclib

-

Paragraph 0018, (2020/09/30)

The invention discloses a preparation me...

Stereoselective N-glycosylation with N4-acyl cytosines and efficient synthesis of gemcitabine

Liu, Tongchao,Tang, Jiadeng,Liang, Jianpeng,Chen, Yabin,Wang, Xiaowen,Shen, Jingkang,Zhao, Dongmei,Xiong, Bing,Cen, Jun-Da,Chen, Yue-Lei

, p. 1203 - 1213 (2019/01/29)

Through systematical comparison of vario...

Synthesis and in vitro activity of N-sulfonylamidine-derived Pyrimidine Analogues

Krstulovi?, Luka,Safti?, Dijana,Ismaili, Hamit,Baji?, Miroslav,Glava?-Obrovac, Ljubica,?ini?, Biserka

, p. 625 - 636 (2018/05/07)

Two novel series of N-sulfonylamidino py...

14631-20-0 Process route

Cytosine
71-30-7

Cytosine

acetic anhydride
108-24-7

acetic anhydride

4-N-Acetylcytosine
14631-20-0

4-N-Acetylcytosine

Conditions
Conditions Yield
With phosphoric acid; at 100 ℃; for 8h;
98%
With pyridine; for 2.5h; Heating;
97.2%
With pyridine; at 20 ℃;
95%
With pyridine; at 20 ℃; for 24h;
85%
In N,N-dimethyl-formamide; for 24h; Ambient temperature;
78%
for 4h; Heating;
75%
 
 
In N,N-dimethyl-formamide;
 
With pyridine;
 
In pyridine;
 
Heating;
 
With pyridine; dmap; In toluene; at 25 - 55 ℃; for 7h;
 
With pyridine; dmap; In toluene; at 25 - 55 ℃; for 7h;
 
With pyridine;
 
4-Amino-1-(2,5-anhydro-β-D-arabinofuranosyl)pyrimidin-2(1H)-one
32830-01-6

4-Amino-1-(2,5-anhydro-β-D-arabinofuranosyl)pyrimidin-2(1H)-one

4-N-Acetylcytosine
14631-20-0

4-N-Acetylcytosine

4-Acetamido-1-(2,3-di-O-acetyl-5-bromo-5-deoxy-β-D-arabinofuranosyl)pyrimidin-2(1H)-one
84856-79-1

4-Acetamido-1-(2,3-di-O-acetyl-5-bromo-5-deoxy-β-D-arabinofuranosyl)pyrimidin-2(1H)-one

4-Amino-1-(5-bromo-5-deoxy-β-D-arabinofuranosyl)pyrimidin-2(1H)-one
58538-06-0

4-Amino-1-(5-bromo-5-deoxy-β-D-arabinofuranosyl)pyrimidin-2(1H)-one

Conditions
Conditions Yield
With hydrogen bromide; In N,N-dimethyl-formamide; at 120 ℃; for 0.416667h;
20%
3%
45%

14631-20-0 Upstream products

  • 71-30-7
    71-30-7

    Cytosine

  • 108-24-7
    108-24-7

    acetic anhydride

  • 3768-18-1
    3768-18-1

    N-acetylcytidine

  • 32830-01-6
    32830-01-6

    4-Amino-1-(2,5-anhydro-β-D-arabinofuranosyl)pyrimidin-2(1H)-one

14631-20-0 Downstream products

  • 136506-88-2
    136506-88-2

    N-[1-(4-Acetylamino-2-oxo-2H-pyrimidin-1-yl)-2,2,2-trichloro-ethyl]-benzamide

  • 141684-80-2
    141684-80-2

    N4-acetyl-1-<5-O-(tert-butyldiphenylsilyl)-3-deoxy-2-Se-phenyl-2-seleno-β-D-erythro-pentofuranosyl>cytosine

  • 136884-09-8
    136884-09-8

    N4-ACETYL-1-[2,2-DIFLUORO-1-[2-(BENZYLOXY)ETHOXY]ETHYL]CYTOSINE

  • 125512-19-8
    125512-19-8

    N4-Acetyl-1-[2,2,2-trifluoro-1-[2-(benzyloxy)ethoxy]ethyl]cytosine